A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5485145



Internal ID262542
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:68009722..68010880hg38UCSC Ensembl
chr10:69769479..69770637hg19UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg381159
hg191159
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17037385
Samples
Known GenesHERC4
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5485145
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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